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NEREIDA ROMERO, MD
MD
Anatomic Pathology & Clinical Pathology Physician
NPI: 1538292289Individual
Specialties, Licenses & Credentials
Anatomic Pathology & Clinical Pathology PhysicianPrimary
Pathology — Anatomic Pathology & Clinical Pathology
Code: 207ZP0102X
041652(GA)ME86441(FL)
Research & Publications (20)
The genome sequence of taurine cattle: a window to ruminant biology and evolution.
PMID 19390049·Science·2009
7-preclinical
A new centronuclear myopathy phenotype due to a novel dynamin 2 mutation.
PMID 19122038·Neurology·2009
5-case
Dynamin 2 mutations associated with human diseases impair clathrin-mediated receptor endocytosis.
PMID 19623537·Hum Mutat·2009
7-preclinical
Are routine radiographs needed in the first year after lumbar spinal fusions?
PMID 19521273·Spine (Phila Pa 1976)·2009
8-other
"Necklace" fibers, a new histological marker of late-onset MTM1-related centronuclear myopathy.
PMID 19084976·Acta Neuropathol·2009
8-other
Differential involvement of sarcomeric proteins in myofibrillar myopathies: a morphological and immunohistochemical study.
PMID 19151983·Acta Neuropathol·2009
8-other
Central role of the oxygen-dependent degradation domain of Drosophila HIFalpha/Sima in oxygen-dependent nuclear export.
PMID 19587118·Mol Biol Cell·2009
7-preclinical
Effect of peers and friends on youth physical activity and motivation to be physically active.
PMID 18617572·J Pediatr Psychol·2009
2-rct
Multigenerational effects in deer mice (Peromyscus maniculatus) exposed to hexahydro-1,3,5-trinitroso-1,3,5-triazine (TNX).
PMID 19230956·Chemosphere·2009
7-preclinical
Four Caucasian patients with mutations in the fukutin gene and variable clinical phenotype.
PMID 19179078·Neuromuscul Disord·2009
5-case
Regulation of the Drosophila hypoxia-inducible factor alpha Sima by CRM1-dependent nuclear export.
PMID 18332128·Mol Cell Biol·2008
7-preclinical
Predicting C-H/pi interactions with nonlocal density functional theory.
PMID 18383059·Chemphyschem·2008
8-other
Study of some physicochemical and functional properties of quinoa (chenopodium quinoa willd) protein isolates.
PMID 18489119·J Agric Food Chem·2008
8-other
Null mutations causing depletion of the type 1 ryanodine receptor (RYR1) are commonly associated with recessive structural congenital myopathies with cores.
PMID 18253926·Hum Mutat·2008
8-other
De novo LMNA mutations cause a new form of congenital muscular dystrophy.
PMID 18551513·Ann Neurol·2008
4-observational
Peroxynitrite inhibits electron transport on the acceptor side of higher plant photosystem II.
PMID 18314005·Arch Biochem Biophys·2008
8-other
Mutations in TPM3 are a common cause of congenital fiber type disproportion.
PMID 18300303·Ann Neurol·2008
8-other
Protein O-mannosyltransferase activities in lymphoblasts from patients with alpha-dystroglycanopathies.
PMID 17869517·Neuromuscul Disord·2008
8-other
Cell autonomy of HIF effects in Drosophila: tracheal cells sense hypoxia and induce terminal branch sprouting.
PMID 18410730·Dev Cell·2008
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 4225 E FOWLER AVE
TAMPA, FL 33617 - Phone
- (813) 972-7100
Quick Facts
- NPI
- 1538292289
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 1
- Publications
- 20
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